KNApSAcK Metabolite C00024693
Metabolite
KNApSAcK Entry
| id | C00024693 |
|---|---|
| Name | Carbazole |
| CAS RN | 86-74-8 |
| Standard InChI | InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H |
| Standard InChI (Main Layer) | InChI=1S/C12H9N/c1-3-7-11-9(5-1)10-6-2-4-8-12(10)13-11/h1-8,13H |
Cluster
| Phytochemical cluster | |
|---|---|
| KCF-S cluster | No. 751 |
Link
ChEMBL
| By standard InChI | CHEMBL243580 |
|---|---|
| By standard InChI Main Layer | CHEMBL243580 |
KEGG
| By LinkDB | C08060 |
|---|
CTD
| By CAS RN | C041514 |
|---|
Species
Summary
List (1)
* NCBI
| KNApSAcK organism | *ID | *family | *plant class | *kingdom |
|---|---|---|---|---|
| Glycosmis pentaphylla Retz.(DC) | 68543 | Rutaceae | rosids | Viridiplantae |
Human Protein / Gene in interaction
5 ChEMBL Protein in interactions
| accession | description | class description | compound | assay ID (# of activities) |
# of diseases
(OMIM / KEGG) |
|---|---|---|---|---|---|
| P00352 | Retinal dehydrogenase 1 | Enzyme | CHEMBL243580 |
CHEMBL1614458
(1)
|
0 / 0 |
| Q99714 | 3-hydroxyacyl-CoA dehydrogenase type-2 | Enzyme | CHEMBL243580 |
CHEMBL1613910
(1)
CHEMBL1614227
(1)
|
3 / 3 |
| P51449 | Nuclear receptor ROR-gamma | Nuclear hormone receptor subfamily 1 group F member 3 | CHEMBL243580 |
CHEMBL2114842
(1)
|
0 / 0 |
| P52732 | Kinesin-like protein KIF11 | Other cytosolic protein | CHEMBL243580 |
CHEMBL1177081
(1)
|
1 / 0 |
| P10275 | Androgen receptor | NR3C4 | CHEMBL243580 |
CHEMBL1794321
(1)
|
3 / 4 |
Related Disease
Diseases related to proteins in ChEMBL interactions
OMIM (7)
| OMIM | preferred title | UniProt |
|---|---|---|
| #300438 | 17-beta-hydroxysteroid dehydrogenase x deficiency |
Q99714
|
| #300068 | Androgen insensitivity syndrome; ais |
P10275
|
| #312300 | Androgen insensitivity, partial; pais |
P10275
|
| #300705 | Mental retardation, x-linked 17; mrx17 |
Q99714
|
| #300220 | Mental retardation, x-linked, syndromic 10; mrxs10 |
Q99714
|
| #152950 | Microcephaly with or without chorioretinopathy, lymphedema, or mental retardation; mclmr |
P52732
|
| #313200 | Spinal and bulbar muscular atrophy, x-linked 1; smax1 |
P10275
|
KEGG DISEASE (7)
| KEGG | disease name | UniProt |
|---|---|---|
| H00024 | Prostate cancer |
P10275
(related)
|
| H00062 | Spinal and bulbar muscular atrophy (SBMA) |
P10275
(related)
|
| H00608 | 46,XY disorders of sex development (Disorders in androgen synthesis or action) |
P10275
(related)
|
| H00609 | 46,XY disorders of sex development (Other) |
P10275
(related)
|
| H00480 | Non-syndromic X-linked mental retardation |
Q99714
(related)
|
| H00658 | Syndromic X-linked mental retardation |
Q99714
(related)
|
| H00925 | 2-Methyl-3-hydroxybutyryl-CoA dehydrogenase (MHBD) deficiency |
Q99714
(related)
|